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Symbol AMMECR1 contributors: mct - updated : 11-10-2017
HGNC name Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1
HGNC id 467
ASSOCIATED DISORDERS
corresponding disease(s) AMME
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS